Attachment of ferrocene nanotubes on beta-cyclodextrin self-assembled monolayers with molecular recognitions

Langmuir. 2004 Sep 28;20(20):8409-13. doi: 10.1021/la049560s.

Abstract

Ferrocene nanotubes were fabricated by binding carboxylic acid-derivatized ferrocenes onto template peptide nanotubes via hydrogen bonding. When these ferrocene-functionalized nanotubes were incubated with beta-cyclodextrin (beta-CD) self-assembled monolayers (SAMs) coated on patterned Au substrates in solution, the ferrocene nanotubes recognized and attached onto the beta-CD SAMs via host-guest molecular recognition. The ferrocene nanotubes were also observed to recognize the certain cavity size of CD. The attachment/detachment of nanotubes on the beta-CD SAMs was controlled electrochemically by tuning the redox states of ferrocene nanotubes. This electric field-responsive building block may be applied to build nanometer-sized switching components in electronics and sensors.

Publication types

  • Letter
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbohydrate Sequence
  • Ferrous Compounds / chemistry*
  • Gold / chemistry
  • Metallocenes
  • Microscopy, Atomic Force
  • Molecular Sequence Data
  • Molecular Structure
  • Nanotubes / chemistry*
  • Peptides / chemistry
  • Silicon / chemistry
  • Surface Properties
  • beta-Cyclodextrins / chemistry*

Substances

  • Ferrous Compounds
  • Metallocenes
  • Peptides
  • beta-Cyclodextrins
  • Gold
  • ferrocene
  • Silicon